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Modafinil

NDC 71610-685 · HUMAN PRESCRIPTION DRUG · TABLET

Generic namemodafinil
Labeler / ManufacturerAphena Pharma Solutions - Tennessee, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA077667
Dosage form / routeTABLET · ORAL
Active ingredientsMODAFINIL (200 mg/1)
Marketing started20140203
Package count2

External sources

Source: openFDA. Public-domain (CC0).